Canonical Allele Identifier: CA684979848

Gene: CDKN1B GPR19

Linked Data

• dbSNP Id: rs879772869
• gnomAD v3: 12-12717639-G-T
• gnomAD v4: 12-12717639-G-T
• MyVariant Identifiers: chr12:g.12870573G>T (hg19) ; chr12:g.12717639G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.12717639G>T , CM000674.2:g.12717639G>T	GRCh38
NC_000012.11:g.12870573G>T , CM000674.1:g.12870573G>T	GRCh37
NC_000012.10:g.12761840G>T	NCBI36
NG_016341.1:g.5272G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000614874.2:c.-201G>T (CDKN1B)	ENSP00000507272.1:n.-201G>T
ENST00000682620.1:n.1631-1186G>T (CDKN1B)
ENST00000684771.1:n.585-1186G>T (CDKN1B)
ENST00000228872.9:c.-201G>T (CDKN1B) MANE Select	ENSP00000228872.4:n.-201G>T
ENST00000228872.8:c.-201G>T (CDKN1B)	ENSP00000228872.4:n.-201G>T
ENST00000477087.1:n.155-1186G>T (CDKN1B)
NM_004064.4:c.-201G>T (CDKN1B)	NP_004055.1:n.-201G>T
XM_011520623.3:c.-2133C>A (GPR19)	XP_011518925.1:n.-2133C>A
XM_017019216.2:c.-2161C>A (GPR19)	XP_016874705.1:n.-2161C>A
NM_004064.5:c.-201G>T (CDKN1B) MANE Select	NP_004055.1:n.-201G>T